Immunotherapy opportunities in ovarian cancer

被引:52
|
作者
Chu, Christina S. [2 ]
Kim, Sarah H. [2 ]
June, Carl H. [3 ]
Coukos, George [1 ]
机构
[1] Univ Penn, Div Gynecol Oncol, Ctr Res Ovarian Canc, Philadelphia, PA 19104 USA
[2] Ctr Res Early Detect & Cure Ovarian Canc, Dept Obstet & Gynecol, Philadelphia, PA 19104 USA
[3] Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
adoptive lymphocyte transfer; antitumor vaccine; B7; CD137; CD40; CTLA-4; cytokines; dendritic cells; DNA vaccine; HER2/neu; hTERT; IFN-alpha; IL-2; monoclonal antibodies; NY-ESO-1; ovarian cancer; p53;
D O I
10.1586/14737140.8.2.243
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ovarian cancer is responsible for the majority of gynecologic cancer deaths and despite the highest standard of multimodality therapy with surgery and cytotoxic chemotherapy, longterm survival remains low. With compelling evidence that epithelial ovarian cancer is an immunogenic tumor capable of stimulating an antitumor immune response, renewed efforts to develop immune therapies to augment the efficacy of traditional therapies are underway. Current immunotherapies focus on varied modes of antitumor vaccine development, particularly with the use of dendritic cell vaccines, effective methods for adoptive T-cell transfer and combinatorial approaches with immune modulatory therapy subverting natural tolerance mechanisms or boosting effector mechanisms. Additional combinatorial approaches include the use of cytokines and/or chemotherapy with immune therapy.
引用
收藏
页码:243 / 257
页数:15
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